A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043211



Internal ID18785742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19906486hg38UCSC Ensembl
Innerchr14:19002112..20374645hg19UCSC Ensembl
Innerchr14:18072112..19444485hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381680852
hg191372534
hg181372374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1753n100
Supporting Variantsnssv3526862
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4K2, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043211
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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